Mattioli Engineering Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K100053 | MATTIOLI PULSE TWO/THREE PLUS FAMILY | March 10, 2010 |
| K042590 | TRANSDERM IONTO SYSTEM, MK 2 | October 14, 2004 |
| K032968 | TRSANSDERM IONTO SYSTEM | December 2, 2003 |
| K965256 | DMS-1000C DERMOABRADER | December 9, 1996 |
| K941838 | MULTIPLE CO2 LAERS | December 15, 1994 |